Primary Device ID | 00815948020481 |
NIH Device Record Key | bf50a27e-5d6a-4cfa-959f-f7870c4144b9 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Indigo |
Version Model Number | CATD-C |
Company DUNS | 191077671 |
Company Name | PENUMBRA, INC. |
Device Count | 1 |
DM Exempt | false |
Pre-market Exempt | false |
MRI Safety Status | Labeling does not contain MRI Safety Information |
Human Cell/Tissue Product | false |
Device Kit | true |
Device Combination Product | false |
Single Use | true |
Lot Batch | true |
Serial Number | false |
Manufacturing Date | false |
Expiration Date | true |
Donation Id Number | false |
Contains Natural Rubber Latex | false |
Labeled No Natural Rubber Latex | true |
RX Perscription | true |
OTC Over-The-Counter | false |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00815948020481 [Primary] |
DXE | Catheter, Embolectomy |
Steralize Prior To Use | true |
Device Is Sterile | true |
[00815948020481]
Ethylene Oxide
[00815948020481]
Ethylene Oxide
[00815948020481]
Ethylene Oxide
[00815948020481]
Ethylene Oxide
[00815948020481]
Ethylene Oxide
[00815948020481]
Ethylene Oxide
[00815948020481]
Ethylene Oxide
[00815948020481]
Ethylene Oxide
[00815948020481]
Ethylene Oxide
[00815948020481]
Ethylene Oxide
[00815948020481]
Ethylene Oxide
[00815948020481]
Ethylene Oxide
[00815948020481]
Ethylene Oxide
[00815948020481]
Ethylene Oxide
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2019-02-04 |
Device Publish Date | 2019-01-03 |
00814548017624 | CATD |
00814548017600 | SEPD |
00815948020481 | Indigo CATD Kit |
00815948022423 | Indigo CATD Kit |
00815948022348 | Aspiration Catheter D Kit |
00815948022331 | Aspiration Catheter D Kit, CE |
00814548019765 | Ind Engine Canister Assembly, CE |
00815948024281 | Indigo CATD Kit |